312 results
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Sources: EU EUDAMED, US FDA
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cobas EGFR Mutation Test V2 Materials number CE-IVD: EGFR v2: 07248563190 cfDNA: 07247737190 Device Identifier: EGFR v2.0: 00875197005448 cfDNA: 00875197005424 Product Usage: A real time PCR Test for the qualitative detection and identifications of mutations n exons 18, 19, 20 and 21 of the epidermal growth factor receptor (EGFR) gene in DNA derived from formalin-fixed paraffin-embedded (FFPET) tumor tissue or plasma from non-small cell lung cancer (NSCLC) patients. The test also is intended to be used as an aid in selecting patients with NSCLC for therapy with an EGFR tyrosine kinase inhibitor (TKI).
FDA Recall
Terminated
·Roche Molecular Systems, Inc.·Product code OWD·April 5, 2016
therascreen PIK3CA RGQ PCR Kit (23) US IVD product- aid clinicians in identifying breast cancer patients who may be eligible for treatment with PIQRAY (alpelisib) based on a PIK3CA Mutation Detected result. REF 873121
FDA Recall
Terminated
·Qiagen Sciences LLC·Product code OWD·December 11, 2020
cobas 4800 KRAS AMP/DET 24T CE-IVD Mutation Test; CE-IVD 5852170190. Intended for the identification of mutations in codons 12,13 and 61 of the KRAS Gene in DNA derived from formalin-fixed paraffin-embedded human colorectal and non-small cell lung cancer tissues.
FDA Recall
Terminated
·Roche Molecular Systems, Inc.·Product code OWD·December 18, 2014
cobas EGFR Mutation Test epidermal growth factor receptor (EGFR) gene DNA assay
FDA Recall
Terminated
·Roche Molecular Systems, Inc.·Product code OWD·January 13, 2015
cobas EGFR Mutation Test, v2 and cobas cfDNA Sample Preparation Hungarian Translation Instructions for Use
FDA Recall
Terminated
·Roche Molecular Systems, Inc.·Product code OWD·March 15, 2016
cobas 4800 BRAF V600 Mutation Test for In Vitro Diagnostic Use Roche Molecular Systems, Inc., Product Usage: The primary use of the cobas 4800 BRAF V600 Mutation Test is the detection of the BRAF V600 mutations in DNA extracted from formalin-fixed, paraffin-embedded human melanoma tissue. It is intended to be used as an aid in selecting melanoma patients whose tumors carry BRAF V600 mutations for treatment with Zelboraf (vemurafenib).
FDA Recall
Terminated
·Roche Molecular Systems, Inc.·Product code OWD·July 31, 2012
VERSYS 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM STR STD BODY/NECK 14X200MM STR STD BODY/NECK REV 13.5X200MM BWD LT 15X200MM STR STD BODY/NECK REV 13.5X200MM BWD RT REV 15.0X200MM BWD LT REV 15.0X200MM BWD RT REV 16.5X200MM BWD LT REV 16.5X200MM BWD RT Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·March 21, 2018
VERSYS 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM STR STD BODY/NECK 14X200MM STR STD BODY/NECK REV 13.5X200MM BWD LT 15X200MM STR STD BODY/NECK REV 13.5X200MM BWD RT REV 15.0X200MM BWD LT REV 15.0X200MM BWD RT REV 16.5X200MM BWD LT REV 16.5X200MM BWD RT Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FDA Recall
Terminated
·Zimmer Biomet, Inc.·Product code LPH·November 29, 2017
PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed bridgework.
FDA Enforcement
Class II
·Terminated·Keystone Dental Inc·March 27, 2013
Segmental fluted stem, 18x250mm bwd, Sterile,
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 21, 2017
Segmental fluted stem, 19x250mm bwd, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 21, 2017
Segmental fluted stem, 16x250mm bwd, Sterile, Knee joint femorotibial meta/polymer constrained cemented prosthesis- Specific Knee, Hip and Nail Implants
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 21, 2017
Segmental fluted stem, 15x250mm bwd, Sterile, Knee joint femorotibial meta/polymer constrained cemented prosthesis- Specific Knee, Hip and Nail Implants
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 21, 2017
Segmental fluted stem, 17x250mm bwd, Sterile, Knee joint femorotibial meta/polymer constrained cemented prosthesis- Specific Knee, Hip and Nail Implants
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 21, 2017
PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed bridgework.
FDA Recall
Terminated
·Keystone Dental Inc·Product code NDP·March 11, 2013
VERSYS 10 INCH BEADED FC REV 13.5X250MM BWD LT and RT VERSYS BEADED FULLCOAT REVISION HIP PROSTHESIS
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·March 21, 2018
VERSYS 10 INCH BEADED FC REV 15.0X250MM BWD LT & RT VERSYS BEADED FULLCOAT REVISION HIP PROSTHESIS
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·March 21, 2018
UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic ultrasound imaging or fluid flow analysis of the human body as Continuous-wave Doppler (CWD) for Cardiac Adult, Cardiac Pediatric, and Peripheral Vessel.
FDA Enforcement
Class II
·Terminated·Hitachi Medical Systems America Inc·February 26, 2020
UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic ultrasound imaging or fluid flow analysis of the human body as Continuous-wave Doppler (CWD) for Cardiac Adult, Cardiac Pediatric, and Peripheral Vessel.
FDA Recall
Terminated
·Hitachi Medical Systems America Inc·Product code ITX·January 31, 2020
Viasys, REF BLD-1000, Pulmanex Adapter 22mm O.D. x 22mm O.D. x 15 mm I.D., manufactured by Unomedical, Inc of McAllen, Texas and assembled in Mexico
FDA Recall
Terminated
·Unomedical, Inc·Product code BZA·December 2, 2004